钝化
材料科学
电解质
硫黄
阴极
锂(药物)
无机化学
锂硫电池
冶金
纳米技术
电极
化学
物理化学
医学
图层(电子)
内分泌学
作者
Walter Cistjakov,Johanna Hoppe,Jinkwan Jung,Fridolin Röder,Hee‐Tak Kim,Ulrike Krewer
标识
DOI:10.1002/admi.202400632
摘要
Abstract One of the remaining challenges for lithium–sulfur batteries toward practical application is early cathode passivation by the insulating discharge product: Li 2 S. To understand how to best mitigate passivation and minimize related performance loss, a kinetic Monte–Carlo model for Li 2 S crystal growth from solution is developed. The key mechanisms behind the strongly different natures of Li 2 S layer growth, structure, and morphology for salts with different (DN) are revealed. LiTFSI electrolyte in dimethyl ether leads to lateral Li 2 S growth on carbon and fast passivation because it increases the Li 2 S precipitation‐to‐dissolution probability on carbon relative to Li 2 S. In contrast, LiBr electrolyte has a higher DN and yields a particle‐like structure due to a significantly higher precipitation‐to‐dissolution probability on Li 2 S compared to carbon. The resulting large number of Li 2 S sites further favors particle growth, leading to low passivation. This study is able to identify the key parameters of the electrolyte and substrate material to tune Li 2 S morphology and growth to pave the way for optimized performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI